Technical Operations Scientist

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在 Kenvue，我們意識到日常護理的非凡力量。我們以一個多世紀的傳統為基礎，植根於科學，是標誌性品牌的品牌 - 包括您已經熟悉和喜愛的 NEUTRGENA®、AVEENO、TYLENOL®®、LISTERINE®、JOHNSON'S® 和 BAND-AID®。科學是我們的熱情所在;關心就是我們的才能。

我們是誰

我們的全球團隊由 ~ 22,000 名才華橫溢的員工組成，他們的職場文化中，每個聲音都很重要，每一個貢獻都受到讚賞。 我們熱衷於洞察， 創新並致力於為我們的客戶提供最好的產品。憑藉專業知識和同理心，成為 Kenvuer 意味著每天有能力影響數百萬人。我們以人為本，熱切關懷，以科學贏得信任，以勇氣解決——有絕佳的機會等著您！加入我們，塑造我們和您的未來。有關更多資訊，請按兩下 here.

Role reports to：

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你會做什麼

Kenvue is currently recruiting for:

Technical Operations Scientist

Who we are At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands - including Neutrogena, Aveeno, Tylenol, Listerine, Johnson’s and BAND-AID® Brand Adhesive Bandages that you already know and love. Science is our passion; care is our talent. Our global team is made up of ~ 22,000 diverse and brilliant people, passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact the life of millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage – and have brilliant opportunities waiting for you! Join us in shaping our future–and yours. For more information, click here.

Role reports to: EMEA Process Science SH&E Cluster Lead

Location: VdR France

Travel %: 10

What you will do

The Technical Operations Scientist is responsible for providing support in Technical Operations for a broad range of consumer cosmetics, OTC drug products, and OTC monograph drug products while developing deeper knowledge and benchmarking with other sites. The Scientist possesses a passion for innovation and continuous improvement. Working under moderate direction, this individual collaborates cross-functionally as needed to provide technical support in the design, development, and implementation of technical solutions for new product introductions, cost reduction and critical initiatives. This individual is expected to implement technical aspects of projects, and interact with multi-functional teams to implement projects.

Key Responsibilities

· Support execution of or lead small to moderately sized project tasks per established timeline, including but not limited to the technology transfer process for New Products Introduction, Product Improvements, and new raw material qualification

· Uses scientific principles to resolve technical challenges while being able to articulate complex subject matter in clear, concise terms. Seeks guidance on more complex technical challenges.

· Support the execution of the planned experimental design (i.e., sample collection, in-process testing, sample management, etc.).

· Prepares technical memos, reports, analyzes and summarizes data, and recommends conclusions based on scientific rationale.

· Support or lead in conducting troubleshooting supply issues, global change control (GCC), root cause analysis, and remediation for technical-related issues]

· Collaborate and work closely with Quality, Operations and R&D teams to ensure seamless transitions through the new product and project development lifecycle.

· Effectively execute technical transfer and life cycle management initiatives

What we are looking for

Required Qualifications

· Bachelor’s Degree is preferred in Pharmacy, Chemistry, Engineering, or related scientific field.

· 2+ years of industry experience related to process development is required.

· Experience within the Consumer and Personal Care industry is preferred. GMP experience is preferred.

Additoinal Requirements

· The Rule requires the presence on Site/shopfloor due to the Operational needs and any remote work needs to be agreed upfront with the Manager

Desired Qualifications

· General knowledge of product characteristics and their correlation with product/raw material performance and performance requirements of specific products or raw materials and the customer needs.

· General knowledge of scientific principles for liquid/semi-solid formulation development

· General understanding of the process equipment and in-process control instruments.

· General process knowledge in a few of the processes such as Mixing, Filling, Liquid dosage, Solid dosage, Liquid Packaging, Scale-up, Technology Transfer, Continued Process Verification, Process Development, as applicable.

· General knowledge of regulatory requirements in the development, validation, and manufacture of consumer cosmetic and OTC monograph drug products (regulatory agencies such as, FDA, MHRA, Health Canada, AIFA etc.).

· Strong analytical skills are required. Excellent technical writing skills are required. Experience with MS Word, Excel and Project software packages is required. Excellent interpersonal, influencing, communication, listening, negotiating and problem-solving/decision-making skills are preferred.

Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment based on business needs, job requirements, and individual qualifications, without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, protected veteran status, or any other legally protected characteristic, and will not be discriminated against on the basis of disability.

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